Novel Indanone Compounds

ABSTRACT

Novel indanylidene compounds can be used as UV-A filters in cosmetic compositions for protecting skin and hair and for technical applications.

FIELD OF THE INVENTION

The invention relates to novel indanylidene compounds, to a process for their preparation and to their use as UVA filters.

BACKGROUND OF THE INVENTION

Indanylidene compounds which have UV-absorbing properties are already known from EP-A 823 418. However, the indanylidene compounds previously described in EP-A 823 418 have a photostability which is too low for the application.

SUMMARY OF THE INVENTION

Novel indanylidene compounds of the formula

in which

-   R¹ to R⁴, independently of one another are hydrogen, C₁-C₂₀ alkyl or     C₅-C₁₀-cycloalkyl, with the proviso that two substituents on     adjacent carbon atoms can together also be an optionally substituted     C₁-C₄-alkylene group; -    may also, independently of one another, be C₂-C₂₀-alkyl, in which     at least one methylene group may be replaced by oxygen,     C₃-C₂₀-alkenyl, C₃-C₂₀-alkinyl or a group S, -    where S may be a silane, an oligosiloxane or a polysiloxane group; -   R⁵ to R⁸, independently of one another, are hydrogen, C₁-C₂₀-alkyl     or C₅-C₁₀-cycloalkyl or C₁-C₂₀-alkoxy, C₅-C₁₀-cycloalkoxy, hydroxyl,     acetoxy, acetamino, carboxyl, carbalkoxy or carbamoyl, -    additionally two substituents of R⁵ to R⁸ on adjacent carbon atoms     can together form a 5-7-membered ring which contains up to three     heteroatoms, where the ring atoms may be substituted by     exocyclically double-bonded oxygen (keto group), -    also, in the case of alkoxy, may, independently of one another, be     C₂-C₂₀-alkyl in which at least one methylene group may be replaced     by oxygen, C₃-C₂₀-alkinyl or a group S, -    where S may be a silane, an oligosiloxane or a polysiloxane group; -   X is cyano, CON(R)₂ or CO₂R, where R is hydrogen or C₁-C₈-alkyl; -   n is 1 or 0; -   R⁹ to R¹¹, in cases where n=1, may be hydrogen, C₁-C₂₀-alkyl or     C₈-C₁₀-cycloalkyl, aryl or heteroaryl, -    additionally two substituents of R⁹ to R¹¹ can, together with the     β-atom from a 3-7-membered ring which may contain up to three     heteroatoms, -    also, in cases where n=0, R⁹ and R¹⁰, together with the β-atom, are     an aryl or heteroaryl radical     have been found.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to novel indanylidene compounds of the formula

in which

-   R¹ to R⁴, independently of one another are hydrogen, C₁-C₂₀-alkyl or     C₅-C₁₀-cycloalkyl, with the proviso that two substituents on     adjacent carbon atoms can together also be an optionally substituted     C₁-C₄-alkylene group; -    may also, independently of one another, be C₂-C₂₀-alkyl, in which     at least one methylene group may be replaced by oxygen,     C₃-C₂₀-alkenyl, C₃-C₂₀-alkinyl or a group S, -    where S may be a silane, an oligosiloxane or a polysiloxane group; -   R⁵ to R⁸, independently of one another, are hydrogen, C₁-C₂₀-alkyl     or C₅-C₁₀-cycloalkyl or C₁-C₂₀-alkoxy, C₅-C₁₀-cycloalkoxy, hydroxyl,     acetoxy, acetamino, carboxyl, carbalkoxy or carbamoyl, additionally     two substituents of R⁵ to R⁸ on adjacent carbon atoms can together     form a 5-7 membered ring which contains up to three heteroatoms, in     particular oxygen or nitrogen, where the ring atoms may be     substituted by exocyclically double-bonded oxygen (keto group), -    also, in the case of alkoxy, may, independently of one another, be     C₂-C₂₀-alkyl in which at least one methylene group may be replaced     by oxygen, C₃-C₂₀-alkenyl, C₃-C₂₀-alkinyl or a group S, -   where S may be a silane, an oligosiloxane or a polysiloxane group; -   X is cyano, CON(R)₂ or CO₂R, where R is hydrogen or C₁-C₈-alkyl; -   n is 1 or 0; -   R⁹ to R¹¹, in cases where n=1, may be hydrogen, C₁-C₂₀-alkyl or     C₅-C₁₀-cycloalkyl, aryl, or heteroaryl, -    additionally two substituents of R⁹ to R¹¹ can, together with the     β-atom form a 3-7-membered ring which may contain up to three     heteroatoms, in particular oxygen or nitrogen, -    also in cases where n=0, R⁹ and R¹⁰, together with the β-atom, are     an aryl or heteroaryl radical.

The novel indanylidene compounds represent a surprising selection from the indanylidene compounds known from EP-A 823 418. They have a significantly higher photostability than the compounds mentioned in EP-A 823 418 and higher compatibility with other UV filters, such as, for example, isooctyl p-methoxycinnamate.

Preference is give to indanylidene compounds of the formula

More preference is given to indanylidene compounds of the formula

Specifically, the following preferred indanylidene compounds may be mentioned:

2-(5,6-Dimethoxy-3,3-dimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanontrile, 2-(5-methoxy-3,3,4,8-tetramethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(3,3,5,6-tetramethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(3,3,6-trimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(5,6-ethylenedioxo-3,3-dimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-(5-methoxy-3,3,6-trimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile, 2-[(5-methoxy-3,3-dimethyl-(2-methyl-3-(1,3,3,3-tetramethyl-1-(trimethyl-silyloxy)-disiloxanyl)-propyl)-indanylidene)]-4,4-dimethyl-3-oxo-pentanonitrile and 2(6-3,3-dimethyl-5-methoxy-1indamylidene)-4,4-dimethyl-3-oxo-pentanonitrile.

The indanylidene compounds according to the present invention can be prepared by (knoevenagel) condensation of compounds of the formula

where

-   R¹ to R⁸ have the meanings given above,     with compounds of the formula     where -   R⁹ to R¹¹ and X have the meanings given above.

The indanones used here can be prepared by Friedel-Crafts Reactions of (substituted) acrylic esters with (substituted) aromatics or, in the case of hydroxyl substituents, by Fries rearrangement of corresponding phenyl esters (F. -H. Marquardt, Helv. Chim. Acta 159, 1476 (1965)).

The preparation of the indanylidene compounds according to the present invention can, for example, be carried out as follows.

The above-mentioned indanones are condensed with equimolar amounts of pivaloylacetonitrile with the catalysis of ammonium acetate according to the conditions of a Knoevenagel condensation.

The preparation can be illustrated by the reaction scheme below.

The indanylidene compounds according to the present invention can be used as UV absorbers, e.g. in cosmetic compositions, in particular for protecting against acute skin damage (sunburn) and also chronic skin damage (premature skin aging), particularly in sunscreen compositions, daily care products and hair care products, but also for improving the photostability of technical products, such as paints, surface coatings, plastics, textiles, packaging materials and rubbers.

The indanylidene compounds according to the present invention can be used individually or in a mixture in the corresponding preparations; it is also possible to use them in combination with UV absorbers of other classes of substance, and also with the latter in any desired mixtures with one another. For example, the following UV absorbers may be mentioned:

-   p-aminobenzoic acid -   ethyl-p-aminobenzoate (25 mol) ethoxylated -   2-ethylhexyl p-dimethylaminobenoate -   ethyl p-aminobenzoate (2 mol) N-propoxylated -   glycerol p-aminobenzoate -   homomethyl salicylate (homosalate) (Neo Heliopan®HMS) -   ethylhexyl salicylate (Neo Heliopan®OS) -   triethanolamine salicylate -   4-isopropylbenzyl salicylate -   menthyl anthranilate (Neo Heliopan®MA) -   ethyl diisopropylcinnamate -   2-ethylhexyl p-methoxycinnamate (Neo Heliopan®AV) -   methyl diisopropylcinnamate -   isoamyl p-methoxycinnamate (Neo Heliopan®E 1000) -   p-methoxycinnamate acid diethanolamine salt -   isopropyl p-methoxycinnamate -   2-ethylhexyl 2-cyano-3,3-diphenyl acrylate (Neo Heliopan®303) -   ethyl 2-cyano-3,3-diphenyl acrylate -   2-phenylbenzimidazolesulfonic acid and salts (Neo Heliopan®hydro) -   3-(4-trimethylammonium)-benzylidene-boman-2-one methylsulfate -   terephthalyidene-dibomanesulfonic acid and salts (Mexoryl®SX) -   4-t-butyl-4′-methoxy-dibenzoylmethane (Avobenzone)/(Neo     Heliopan®357) -   β-imidazole-4(5)-acrylic acid (Urocanic acid) -   2-hydroxy-4-methoxybenzophenone (Neo Heliopan®BB) -   2-hydroxy-4-methoxybenzophenone-5-sulfonic acid -   dihydroxy-4-methoxybenzophenone -   2,4-dihydroxybenzophenone -   tetrahydroxybenzophenone -   2,2′-dihydroxy-4,4′-dimethoxybenzophenone -   2-hydroxy-4-n-octoxybenzophenone -   2-hydroxy-4-methoxy-4′-methylbenzophenone -   3-(4′-sulfo)benzylidene-boman-2-one and salts -   3-(4′-methylbenzylidene)-d.I-camphor (Neo Heliopan®MBC) -   3-benzylidene-d,I-camphor -   4-isopropyldibenzoylmethane -   2,4,6-trianilino-(p-carbo-2′-ethylhexyl-1′-oxy)-1,3,5-triazine -   phenylene-bis-benzimidazyl-tetrasulfonic acid disodium salt (Neo     Heliopan®AP) -   2,2-(1,4-phenylene)-bis-(1H-benzimidazole-4,6-disulfonic acid),     monosodium salt -   N-[(2 and 4)-[2-(oxoborn-3-ylidene)methyl]benzyl]-acrylamide-polymer -   phenol,     2-(2H-benzotriazol-2-yl)-4-methyl-6-(2-methyl-3(1,3,3,3-tetramethyl-1-(trimethylsilyl)-oxy)-disiloxyanyl)-propyl),     (Mexoryl®XL) -   bis-(2-ethylhexyl) 4,4′-[(6-[4-(1,1-dimethyl)-aminocarbonyl)-     phenylamino]-1,3,5-triazine-2,4-diyl)dimino]-bis-(benzoate)     (Uvasorb®HEB) -   2,2′-methylene-bis-(6-(2H-benztriazol-2-yl)-4-1,1,3,3-tetramethylbutyl)-phenol),     (Tinosorb®M) -   2,4-bis-[4-(2-ethylhexyloxy)-2-hydroxyphenyl]-1,3,5-triazine -   benzylidene malonate-polysiloxane (Parsol®SLX) -   glycerylethyl hexanoate-dimethoxycinnamate -   disodium 2,2′-dihydroxy-4,4′-dimethoxy-5,5′-disulfo-benzophenone -   dipropylene glycol salicylate -   sodium hydroxymethoxybenzophenonesulfonate -   tris (2-ethylhexyl)     4,4′,4-(1,3,5-triazine-2,4,6-triyltriimino)-tris-benzoate     (Uvinul®T150) -   2,4-bis-[{(4-(2-ethyl-hexyloxy)-2-hydroxy}-phenyl]-6-(4-methoxyphenyl)-1,3,5-triazine     (Tinosorb®S) -   2,4-bis-[{(4-(3-sulfonato)-2-hydroxy-propyloxy)-2hydroxy}-phenyl]-6-(4-methoxyphenyl)-1,3,5-triazine     sodium salt -   2,4-bis-[{(4-(2-ethyl-hexyloxy)-2-hydroxy}-phenyl]-6-[4-(2-methoxyethyl-carbonyl)-phenylamino]-1,3,5-triazine -   2,4-bis-[{(4-(3-(2-propyloxy)-2-hydroxy-propyloxy)-2-hydroxy}-phenyl]-6-[4-(2-ethylcarboxyl)-phenylamino]-1,3,5-triazine -   2,4-bis-[{(4-(2-ethyl-hexyloxy)-2-hydroxy}-phenyl]-6-(1-methyl-pyrrol-2-yl-)-1,3,5-triazine -   2,4-bis-[{4-tris-(trimethylsiloxy-silylpropyloxy)-2-hydroxy}-phenyl]-6-(4-methoxyphenyl)-1,3,5-triazine -   2,4-bis-[{4-(2″-methylpropenyloxy)-2-hydroxyl}-phenyl]-8-(4-methoxyphenyl)-1,3,5-triazine -   2,4-bis-[{4-(1′,1′,1′3′5′,5′,5′-heptamethylsiloxy-2″-methyl-propyloxy)-2-hydroxy}-phenyl]-6-(4-methoxyphenyl)-1,3,5-triazine

Particularly suitable UV absorbers are:

-   p-aminobenzoic acid -   3-(4′-trimethylammonium)-benzylidene-boman-2-one methylsulfate -   homomethyl salicylate (Neo Heliopan®HMS) -   2-hydroxy-4-methoxy-benzophenone (Neo Heliopan®BB) -   2-phenylbenzimidazolesulfonic acid (Neo Heliopan®Hydro) -   terephthalylidenedibornanesulfonic acid and salts (Mexoryl®SX) -   4-tert-butyl-4′-methoxydibenzoylmethane (Neo Heliopan®357) -   3-(4′-sulfo)benzylidene-boman-2-one and salts -   2-ethylhexyl 2-cyano-3,3-diphenylacrylate (Neo Heliopan®303) -   N-[(2 and 4)-[2-(oxoborn-3-ylidene)methyl]benzyl]-acryulamide     polymer -   2-ethylhexyl p-methoxycinnamate (Neo Heliopan®AV) -   ethyl p-aminobenzoate (25 mol) ethoxylated -   isoamyl p-methoxycinnamate (Neo Heliopan®E1000) -   2,4,6-trianilino-(p-carbo-2′-ethylhexyl-1′-oxy)-1,3,5-triazine     (Uvinul®T150) -   phenol,     2-(2H-benzotriazol-2-yl)-4-methyl-6-(2-methyl-3(1,3,3,3-tetramethyl-1-(trimethylsilyl)-oxy)-disiloxyanyl)-propyl),     (Mexoryl®XL) -   bis-(2-ethylhexyl)     4,4′-[(6-[4-(1,1-dimethyl)-aminocarbonyl)-phenylamino]-1,3,5-triazine-2,4-diyl)-diimino]-bis-(benzoate),     (UvasorbHEB) -   3-(4′-methylbenzylidene)-d,I-camphor (Neo Heliopan®MBC) -   3-benzylidenecamphor -   2-ethylhexyl salicylate (Neo Heliopan®OS) -   2-ethylhexyl 4-dimethylaminobenzoate (Padimate O) -   hydroxy-4-methoxybenzophenone-5-sulfonic acid and Na salt -   2,2′-methylene-bis-(6-(2H-benztriazol-2-yl)-4-1,1,3,3-tetramethylbutyl)-phenol),     (Tinosorb®M) -   phenylene-bis-benzimidazyltetrasulfonic acid disodium salt (Neo     Heliopan®AP) -   2,4-bis-[{(4-(2-ethyl-hexyloxy)-2-hydroxy}-phenyl]-6-(4-methoxyphenyl)-1,3,5-triazine,     (Tinosorb®S) -   benzylidene malonate-polysiloxane (Parsol®SLX) -   menthyl anthranilate (Neo Heliopan®MA)

It may also be advantageous to use polymer-bonded or polymeric UV absorbers in preparations according to the present invention, in particular those described in WO-A-92/20690. The combination of the indanylidene compounds according to the present invention with finely divided inorganic and organic pigments, such as, for example, titanium dioxide, zinc oxide and iron oxide and Tinosorb®M, in sunscreen and daily care products with UV protection is likewise possible.

The list of UV filters given which can be used for the purposes of the present invention is not of course intended to be limiting.

The total amount of all (mono- and polysulfonated) water-soluble UV filter substances in the finished cosmetic or dermatological preparations, for example of phenylene-bis-benzimidazyl-tetrasulfonic acid disodium salt or salts thereof and/or the corresponding disulfonic acid or salts thereof and/or 2-phenylbenzimidazole-5-sulfonic acid and salts thereof and/or 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid and salts thereof and/or 4-(2-oxo-3-bomylidenemethyl)-benzenesulfonic acid and salts thereof and/or 2-methyl-5-(2-oxo-3-bornylidene-methyl)-benzenesulfonic acid and salts thereof and/or benzene-1,4-di-(2-oxo-3-bornylidenemethyl)-10-sulfonic acid and salts thereof, is advantageously chosen from the range from 0.1 to 10.0% by weight, preferably 0.6 to 6.0% by weight, based on the total weight of the preparations, if the presence of these substances is desired.

The total amount of oil-soluble UV filter substances in the finished cosmetic or dermatological preparations, for example of tris(2-ethylhexyl) 4,4′,4″-(1,3,5-triazine-2,4,6-triyltriimino)-tris-benzoate and/or 4-tert-butyl-4′-methoxy-dibenzoylmethane and/or 4-methylbenzylidenecamphor and/or octyldimethyl-p-aminobenzoic acid and/or Mexoryl®XL and/or Uvasorb®HEB and/or Tinosorb®S and/or benzophenone-3 and/or Parsol®SLX and/or Neo Heliopan®MA is advantageously chosen from the range from 0.1 to 10.0% by weight, preferably 0.5 to 6.0% by weight, based on the total weight of the preparations, if the presence of these substances is desired.

The total amount of 2-ethylhexyl p-methoxycinnamate and/or isoamyl p-methoxycinnamate in the finished cosmetic or dermatological preparations is advantageously chosen from the range from 0.1 to 15.0% by weight, preferably 0.5 to 7.5% by weight, based on the total weight of the preparations, if the presence of these substances is desired.

The total amount of ethylhexyl 2-cyano-3,3-diphenylacrylate in the finished cosmetic or dermatological preparations is, if the presence of this substance is desired, advantageously chosen from the range from 0.1 to 15.0%, preferably 0.5 to 10.0% by weight, based on the total weight of the preparations.

The total amount of one or more salicylic acid derivatives in the finished cosmetic or dermatological preparations is advantageously chosen from the range from 0.1 to 15.0% by weight, preferably 0.5 to 10.0% by weight, based on the total weight of the preparations. If ethylhexyl salicylate is chosen, it is advantageous to choose its total amount from the range from 0.1 to 5.0% by weight. If homomenthyl salicylate is chosen, it is advantageous to choose its total amount from range from 0.1 to 10.0% by weight.

The indanylidene compounds according to the present invention are also suitable to a particular degree for photostabilizing UV absorbers with low UV photostability. The photostabilization of the very photo-unstable compounds of the dibenzoylmethane, e.g. tert-butyl-4′-methoxydibenzoyl-methane, is particularly successful.

A further photostable UV filter combination is achieved using 0.1 to 10% by weight, preferably 1 to 10% by weight, of ethylhexyl p-methoxycinnamate or isoamyl p-methoxy cinnamate with 0.1 to 10% by weight, preferably 1 to 6% by weight, of the compound of the formula I, preferably in the ratio 1:1.

The combinations of p-methoxycinnamic esters and dibenzoylmethane derivatives and compounds of the formula I can be formulated to be photostable by using, for example, 0.1 to 5% by weight, preferably 1 to 3% by weight, of 4-tert-butyl-4′-methoxydibenzoyl-methane, 0.1 to 10% by weight, preferably 1 to 7.5% by weight of ethylhexyl p-methoxycinnamate or isoamyl p-methoxycinnamate and at least 0.2% by weight, preferably 1 to 6% by weight, of the compounds of the formula I, preferably in the ratio 1 part of dibenzoylmethane derivative, 2 parts p-methoxycinnamic ester and 2 parts of the indanylidene compounds according to the invention.

In addition, it is advantageous to add one or more very photostable UV absorbers to this three-way combination, such as, for example, methylbenzyldenecamphor, 2-ethylhexyl 2-cyano-3,3′-diphenylacrylate, octyltriazone, Uvasorb®HEB, Tinosorb®S, Tinosorb®M, ethylhexyl salicylate, homomenthyl salicylate, and phenylenebisimidazolesulfonic acid or phenylene-bis-benzimidazole-tetrasulfonic acid disodium salt, Mexoryl®SX, Mexoryl®XL or Parsol®SLX.

In addition, in cosmetic preparations, a synergistic increase in the sun protection factor is surprisingly achieved using indanylidene derivatives of the formula I in combination with other UV filters. Examples of a synergistic increase in the sun protection factor are cosmetic emulsions which comprise both a compound of the formula I and also ethylhexyl methoxycinnamate or octocrylene, or a combination of a compound of the formula I with ethylhexyl methoxycinnamate and 2-phenylbenzimidazolesulfonic acid, or ethylhexyl methoxycinnamate and methylbenzylidenecamphor, or ethylhexyl methoxycinnamate and 4-t-butyl-4′-methoxydibenzoylmethane, or Neo Heliopan®AP and ethylhexyl methoxycinnamate, or a combination of a compound of the formula I with octocrylene, methylbenzylidenecamphor and zinc oxide. Combinations of a compound of the formula I with dibenzoylmethanes, methylbenzylidenecamphor, 2-phenylbenzimidazolesulfonic acid, Neo Heliopan®AP, Mexoryl®SX, Mexoryl®XL, Parsol®SLX, Tinosorb®S, Tinosorb®M, Uvinul®T150, Uvasorb®HEB, and microfine pigments, zinc oxide and titanium oxide, also have synergistic increases in the sun protection factors. Such UV filter combinations are listed by way of example, and are not to be understood as being limited to the above-mentioned combinations. Thus, it is possible to use combinations of all UV absorbers already mentioned as particularly suitable on pages 8/9, and UV filters approved in the subsequent publications with compounds of the formula I or the above-mentioned combinations, individually or in any desired mixtures.

-   USA: Food and Drug Administration (FDA). Publication in monograph     for Sunscreen Drug Products for Over-The-Counter Human Use. -   Europe: EC Directive 76/768 of the Council for adapting the legal     provisions of the member states regarding cosmetic compositions to     technical progress. Publications in the Official Journal of European     Communities. -   Japan: Publication of the Cosmetics Directive of the Ministry of     Health and Welfare (MHW). -   Germany: Publication in the Verordnung über kosmetische Mittel     [Directive concerning cosmetic compositions] according to the     Lebensmittel- und Bedarfsgegenstände-Gesetz (LMBG) [Act relating to     Foods and Commodities]. -   Australia: Registration by Therapeutic Goods Administration (TGA)     and publication in the Australian Register of Therapeutic Goods     (ARTG).

These combinations usually achieve a synergistic increase in the UV sun protector factor.

The combination of compounds of the formula I with UV-A absorbers, particularly UV-A-II absorbers, gives broad protection against UV-A radiation (320-400 nm). In particular, a combination of compounds of the formula I with Neo Heliopan®AP (UV-AII absorber) is to be mentioned for broad UV-A protection performances. Further, UV-A filters which are used in combination with compounds of the formula I alone or in combination of compounds of the formula I and Neo Heliopan®AP are Mexoryl®SX, Mexoryl®XL, Tinosorb®M, Tinosorb®S, benzophenone-3, benzophenone-4, Neo Heliopan®357, Neo Heliopan®MA.

For optimum broad-band protection against UV-A and UV-B radiation, the above-mentioned combinations are to be combined with all UV-B filters and mixtures of these filters (cf. list on pages 6-9). Preferably suitable are Neo Heliopan®AV, Neo Heliopan®E1000, Neo Heliopan®Hydro, Neo Heliopan®MBC, Neo Heliopan®303, Neo Heliopan®OS, Neo Heliopan®HMS, Uvinul®T150, Uvasorb®HEB, ethylhexyl dimethylaminobenzoate.

Combining compounds of the formula I with Neo Heliopan®AP and a UV-B filter, e.g. ethylhexyl methoxycinnamate or UV-B filter mixtures, and coated or uncoated finely disperse metal oxides, such as, for example, zinc oxide, titanium dioxide, achieves UV broad-band protection performance with a critical wavelength λ_(amt) of >380 nm (cf. Diffey in Int. J. Cosm. Science 16, 47 (1994)).

Furthermore, the indanylidene compounds according to the present invention can be combined alone or with other UV absorbers used for the protection of technical products.

Examples of such UV absorbers are compounds from the series of benzotriazoles, benzophenones, triazones, cinnamic esters and oxalanilides.

The indanylidene compounds according to the present invention are crystalline and have to be dissolved sufficiently in cosmetic preparation to avoid the probelm of recrystallization following a prolonged storage period. A sufficient amount of the oil components customarily used in cosmetic preparations, liquid oil-soluble UV absorbers or alcohols, e.g. ethanol, isopropanol or 1-butanol, is necessary to avoid recrystallization. More preference is given to the use of the following oil components and/or UV absorbers for achieving adequate solubility of combinations of the indanylidene compounds according to the present invention: ethylhexylmethoxycinnamate, isoamyl methoxycinnamate, octocrylene, ethylhexyl salicylate, homosalate, menthyl anthranilate, padimate O, diisopropyl adipate, C₁₂₋₁₅alkyl benzoate (Witconol TN), butylene glycol dicaprylate/dicaprate (Miglyol 8810), cocoglycerides (Myritol 331), caprylic/capric triglycerides (Miglyol 312), cetearyl isononanate (Cetiol SN), PVP/hexadecane copolymer (Unimer U151), adipic acid/diethylene glycol/isononanoic acid copolymer (Lexorez 100), propylene glycol dicaprylate/dicaprate (Myritol PC), hexyl laurate (Cetiol A), dicapryl ether (Cetiol OE), diethylhexyl naphthalate (Hallbrite®TQ), butyloctyl salicylate (Hallbrite®BHB), dibutyl adipate (Cetiol B), triethyl citrate (hydragen CAT), propylene glycol dibenzoate (Finsolv PG 22), tributyl citrate, dioctyl malate (Ceraphyl 45), dipropylen glycol dibenzoate (Benzoflex 245), acetyltributyl citrate (Citroflex A-4), acetyl/triethyl citrate (Citroflex A-2). The list of the oils which can be used for the purposes of the present invention is not of course intended to be limiting.

The use amount of all oil components in cosmetic emulsions with compounds of the formula is 0.5 to 30% by weight, preferably 2 to 15% by weight. All said oil components and liquid oil-soluble UV filters are excellent solvents for all crystalline oil-soluble UV absorbers.

It is a serious drawback if UV absorbers leave behind marks which cannot be washed out of items of clothing. In particular, it is known that the UV-A absorber tert-butylmethoxydibenzoylmethane produces marks on textiles which cannot be washed out. The indanylidene compounds according to the present invention do not have this drawback since a mark formed on textiles can be very readily washed out.

Sunscreen products should be water-resistant in order that sufficient UV protection is ensured for the user, in particular children, while swimming or bathing. Combinations of the indanylidene compounds according to the present invention satisfy these requirements to a particularly good degree. In an O/W emulsion containing 3% by weight of a combination of the indanylidene compounds according to the present invention, 97% substantivity of the UV absorber was measured following washing, and in a W/O emulsion, 95%. Furthermore, the water resistance of sun protection products containing water-soluble, mono- or polysulfonated UV filters, such as, for example, Neo Heliopan®AP, Maxoryl®SX, benzophenone-4, Neo Heliopan®Hydro and the oil-soluble UV absorbers listed on pages 6-9 can be significantly increased as a result of combination with compounds of the formula I.

It may also be of considerable advantage to combine the UV absorbers mentioned according to the present invention with chelating substances, as are listed, for example, in EP-A 313 305 and WO-94/04128, or with polyaspartic acid and ethylenediamine-tetramethyl-phosphonic acid salts.

Cosmetic dermatological formulations for the purposes of the present invention comprise one or more customary UV-A, UV-B and/or broad-band filters as individual substances or in any mixtures with one another, in the lipid phase and/or in the aqueous phase. They are satisfactory products in every respect which are surprisingly characterized by high UV-A protection performance and high sun protection factor.

The present invention further provides for the use of the UV absorbers according to the present invention in combination with conventional UV absorbers for enhancing the protection against harmful UV radiation beyond the extent of the protection achieved using the same amounts of conventional or of UV filters according to the present invention on their own (synergistic effect).

The total amount of UV filter substances (UV-A, UV-B and/or broad-band filters) in the finished cosmetic or dermatological preparations, whether as individual substance or in any mixtures with one another, is advantageously chosen from the range from 0.1 to 30% by weight, preferably 0.1 to 10.0% by weight, more preferably 0.5 to 5.0% by weight, based on the total weight of the preparations.

In addition, cosmetic and dermatological preparations according to the present invention advantageously, but not obligatorily, comprise inorganic pigments based on finely disperse metal oxides and/or other metal compounds which are insoluble or sparingly soluble in water, in particular the oxides of titanium (TiO₂), zinc (ZnO), iron (e.g. Fe₂O₃), zirconium (ZrO₂), silicon (SiO₂), manganese (e.g. MnO), aluminum (A1₂O₃), cerium (e.g. Ce₂O₃), mixed oxides of the corresponding metals, and mixtures of such oxides. These pigments are X-ray-amorphous or non-X-ray-amorphous. More preference is given to pigments based on TiO₂. X-ray-amorphous oxide pigments are metal oxides or semi-metal oxides which reveal no or no recognizable crystalline structure in X-ray diffraction experiments. Such pigments are often obtainable by flame reaction, for example by reacting a metal or semi-metal halide with hydrogen and air (or pure oxygen) in a flame.

In cosmetic, dermatological or pharmaceutical formulations, X-ray-amorphous oxide pigments are used as thickeners and tixotropic agents, flow auxiliaries for emulsion and dispersion stabilization and as carrier substance (for example for increasing the volume of finely divided powders). X-ray-amorphous oxide pigments which are known and often used in cosmetic or dermatological galerics are, for example, high-purity silicon oxide. Preference is given to high-purity, X-ray-amorphous silicon dioxide pigments with a particle size in the range from 5 to 40 nm and an active substance (BET) in the range from 60 to 400 m²/g, preferably 150 to 300 m²/g, where the particles are to be regarded as spherical particles of very uniform dimension. Macroscopically, the silicon dioxide pigments are recognizable as loose, white powders. Silicon dioxide pigments are sold commercially under the name Aerosil® (CAS-No. 7631-85-9) or Carb-O-Sil.

Advantageous Aerosil® grades are, for example, Aerosil®0X50, Aerosil®130, Aerosil®150, Aerosil®200, Aerosil®300, Aerosil®380, Aerosil®MQX 80, Aerosil® MOX 170, Aerosil®COK 84, Aerosil® R 202, Aerosil®R 805, Aerosil®R 812, Aerosil®R 972, Aerosil®R 974, Aerosil®R978.

According to the present invention, cosmetic or dermatological light protection preparations comprise 0.1 to 20% by weight, advantageously 0.5 to 10% by weight, more preferably 1 to 5% by weight, of X-ray-amorphous oxide pigments.

The non-X-ray-amorphous inorganic pigments are, according to the present invention, advantageously in hydrophobic form, i.e. have been surface-treated to repel water. This surface treatment may involve providing the pigments with a thin hydrophobic layer by processes known per se. Such a process involves, for example, producing the hydrophobic surface layer by a reaction according to n TiO₂ +m (RO)₃Si—R′→n TiO₂ (surf.) where n and m are stoichiometric parameters to be used as desired, and R and R′ are the desired organic radicals. Hydrophobicized pigments prepared analogously to DE-A 33 14 742, for example, are advantageous.

For example, mention may be made of TiO₂ pigments, as are sold under the tradename T805 from Degussa. Preference is also given to TiO₂Fe₂O₃ mixed oxides, as are supplied, for example, under the trade name T817, also from Degussa.

The total amount of inorganic pigments, in particular hydrophobic inorganic micropigments, in the finished cosmetic or dermatological preparations is advantageously chosen from the range from 0.1 to 30% by weight, preferably 0.1 to 10.0% by weight, preferably 0.5 to 6.0% by weight, based on the total weight of the preparations.

The cosmetic and/or dermatological formulations according to the present invention can have the customary composition and can be used for cosmetic and/or dermatological sun protection, and also for the treatment, care and cleansing of the skin and/or of the hair and as a make-up product in decorative cosmetics. Accordingly, the preparations according to the present invention can, depending on their formulation, be used, for example, as skin protection cream, cleansing milk, sunscreen lotion, nourishing cream, day cream or night cream, etc. In some instances, it is possible and advantageous to use the preparations according to the present invention as bases for pharmaceutical formulations. Preference is given, in particular, to those cosmetic and dermatological preparations in the form of a skin care or make-up product. Typical embodiments are creams, gels, lotions, alcoholic and aqueous/alcoholic solutions, emulsions or stick preparations. These compositions may also comprise, as further auxilaries and additives, mild surfactants, co-emulsifiers, superfatting agents, pearlescent waxes, bodying agents, thickeners, polymers, silicone compounds, fats, waxes, stabilizers, biogenic active ingredients, deoderant active ingredients, antidandruff agents, film formers, swelling agents, hydrotropic agents, preservatives, insect repellants, tanning agents, artificial self-tanning agents (e.g. dihydroxyacetone), stabilizers, perfume oils, dyes, antimicrobial agents and the like.

For use, the cosmetic and dermatological preparations according to the present invention are applied to the skin and/or the hair in a sufficient amount in the manner customary for cosmetics.

More preference is given to those cosmetic and dermatological preparations in the form of a cosmetic composition for the protection of the skin and hair. Advantageously, in addition to UV-A, UV-B and/or broad-band filters used according to the present invention, these can contain at least one inorganic pigment, preferably an inorganic micropigment.

The cosmetic and dermatological preparations according to the present invention can comprise cosmetic auxiliaries, as are customarily used in such preparations, e.g. preservatives, bactericides, perfumes, antifoams, dyes, pigments which have a coloring action, thickeners, moisturizers and/or humectants, fats, oils, waxes or other customary constituents of a cosmetic or dermatological formulation, such as alcohols, polyols, polymers, foam stabilizers, electrolytes, organic solvents or silicone derivatives. Suitable nonionic emulsifiers or dispersants are the group formed by polyglyceryl-2-dipolyhydroxystearate (Dehymuls®PCPH), polyglyceryl-3-diisostearate (Lameform®TGI), polyglyceryl-4 isostearate (Isolan®GI 34), polyglyceryl-3 oleate, diisostearyl polyglyceryl-3 diisostearate (Isolan®PDI), polyglyceryl-3 methylglucose distearate (Tego Carey® 450), polyglyceryl-3 beeswax (Cera Bellina®), polyglyceryl-4 caprate (polyglycerol caprate T2010/90), polyglyceryl-3 catyl ether (Chimexane®NL), polyglyceryl-3 distearate (Cremophor®GS 32), polyglyceryl-2 stearate (Hosfacerin®DGMS) and polyglyceryl polyricineoleate (Admul®WOL 1403), and mixtures thereof.

The amounts of cosmetic or dermatological auxiliaries and carrier substances and perfume which can be used in each case can be determined easily by the person skilled in the art by simple trial and error, depending on the nature of the product in question.

An additional content of antioxidants is generally preferred. According to the present invention, favorable antioxidants which can be used ar all antioxidants customary or suitable for cosmetic and/or dermatological applications.

The antioxidants are advantageously chosen from the group of amino acids (e.g. glycine, histidine, tyrosine, tryptophan) and derivatives thereof, imidazoles (e.g. urocanic acid) and derivatives thereof, peptides, such as D,L-carnosine, D-carnosine, L-carnosine, and derivatives thereof (e.g. anserine), carotenoids, carotenes, (e.g. α-carotene, β-carotene, lycopene) and derivatives thereof, chlorogenic acid and derivatives thereof, lipoic acid and derivatives thereof (e.g. dihydrolipoic acid), aurothioglucose, propylthiouracil and other thiols (e.g. thioredoxin, glutathione, cysteine, cystine, cystamine and the glycosyl, N-acetyl, methyl, ethyl, propyl, amyl, butyl and lauryl, palmitoyl, oleyl, γ-linoleyl, chotesteryl and glyceryl esters thereof) and salts thereof, dilauryl thiodipropionate, distearyl thiodipropionate, thiodipropionic acid and derivatives thereof (esters, ethers, peptides, lipids, nucleotides, nucleosides and salts), and sulfoximine compounds (e.g. buthionine sulfoximines, homocysteine sulfoximine, buthionine sulfones, penta-, hexa-, heptathionine sulfoximine) in very low tolerated doses (e.g. pmol to μmol/kg), and also (metal) chelating agents (e.g. α-hydroxy fatty acids, palmitic acid, phytic acid, lactoferrin), α-hydroxy acids (e.g. citric acid, lactic acid, maleic acid), humic acid, bile acid, bile extracts, bilirubin, bilivardin, EDTA, EGTA and derivatives thereof, unsaturated fatty acids and derivatives thereof (e.g. γ-linolenic acid, linoleic acid, oleic acid), folic acid and derivatives thereof, ubiquinone and ubiquinol and derivatives thereof, vitamin C and derivatives (e.g. ascorbyl palmitate, Mg ascorbyl phosphate, ascorbyl acetate), tocopherols and derivatives (e.g. vitamin E acetate), vitamin A and derivatives (vitamin A palmitate), and coniferyl benzoate of benzoin resin, rutinic acid and derivatives thereof, α-glycosylrutin, ferulic acid, furfurylideneglucitol, carnosine, butylhydroxytoluene, butylhydroxyanisol, nordihydroguaiacic acid, nordihydrogualaretic acid, trihydroxybutyrophenone, uric acid and derivatives thereof, mannose and derivatives thereof, zinc and derivatives thereof (e.g. ZnO, ZnSO₄), selenium and derivatives thereof (e.g. selenomethionine), stilbenes and derivatives thereof (e.g. stilbene oxide, trans-stilbene oxide) and the derivatives (salts, esters, ethers, sugars, nucleotides, nucleosides, peptides and lipids) of the active ingredients suitable according to the present invention.

The amount of the above-mentioned antioxidants (one or more compounds) in the preparations is preferably 0.001 to 30% by weight, more preferably 0.05 to 20% by weight, and most preferably 1 to 10% by weight, based on the total weight of the preparation.

If vitamin E and/or derivatives thereof represent the antioxidant(s), it is advantageous to choose their respective concentrations from the range from 0.001 to 10% by weight, based on the total weight of the formulation.

If vitamin A or vitamin A derivatives, or carotenes or derivatives thereof represent the antioxidant(s), it is advantageous to choose their respective concentrations from the range from 0.001 to 10% by weight, based on the total weight of the formulation.

The lipid phase can advantageously be chosen from the following group of substances:

-   -   mineral oils, mineral waxes;     -   oils, such as triglycerides of capric or of caprylic acid, and         also natural oils, such as, for example, castor oil;     -   fats, waxes and other natural and synthetic fatty substances,         preferably esters of fatty acids with alcohols of low carbon         number, e.g. with isopropanol, propylene glycol or glycerol, or         esters of fatty alcohols with alkanoic acids of low carbon         number or with fatty acids;     -   alkyl benzoate;     -   silicone oils, such as dimethylpolysiloxane,         diethylpolysiloxane, diphenylpolysiloxane, and mixed forms         thereof.

The oil phases of the emulsions, oleogels and hydrodispersions or lipodispersions for the purposes of the present invention are advantageously chosen from the group of esters of saturated and/or unsaturated, branched and/or unbranched alkanecarboxylic acids having a chain length of from 3 to 30 carbon atoms and saturated and/or unsaturated, branched and/or unbranched alcohols having a chain length of from 3 to 30 carbon atoms, from the group of esters of aromatic carboxylic acids and saturated and/or unsaturated, branched and/or unbranched alcohols having a chain length of from 3 to 30 carbon atom. Such ester oils can then advantageously be chosen from the group isopropyl myristate, isopropyl palmitate, isopropyl stearate, isopropyl oleate, n-butyl stearate, n-hexyl laurate, n-decyl oleate, isooctyl stearate, isononyl stearate, isononyl isononanate, 2-ethylhexyl palmitate, ethylhexyl laurate, 2-hexyldecyl stearate, 2-octyldodecyl palmitate, oleyl oleate, oleyl erucate, erucyl oleate and synthetic, semisynthetic and natural mixtures of such esters, e.g. jojoba oil.

In addition, the oil phase can advantageously be chosen from the group of branched and unbranched hydrocarbons and hydrocarbon waxes, silicone oils, dialkyl ethers, the group of saturated or unsaturated, branched or unbranched alcohols, and fatty acid triglycerides, namely the triglycerol esters saturated and/or unsaturated, branched and/or unbranched alkanecarboxylic acids having a chain length of from 8 to 24, in particular 12 to 18, carbon atoms. The fatty acid triglycerides can, for example, advantageously be chosen from the group of synthetic, semisynthetic and natural oils, e.g. olive oil, sunflower oil, soybean oil, peanut oil, rapeseed oil, almond oil, palm oil, coconut oil, palm kernel oil and the like.

Any mixtures of such oil and wax components are also to be used advantageously for the purposes of the present invention. It may also be advantageous in some instances to use waxes, for example cetyl palmitate, as the sole lipid component of the oil phase.

The oil phase is advantageously chosen from the group 2-ethylhexyl isostearate, octyldodecanol, isotridecyl isononanoate, isosicosane, 2-ethylhexyl cocoate, C₁₂₋₁₈-alkyl benzoate, caprylic/capric trilyceride, dicapryl ether.

Particularly advantageous mixtures are those of the C₁₂₋₁₅-alkyl benzoate and 2-ethylhexyl isostearate, those of C₁₂₋₁₅-alkyl benzoate and isotridecyl isononanoate, those of the C₁₂₋₁₅-alkyl benzoate, 2-ethylhexyl isostearate and isotridecyl isononanoate.

The oil phase can also advantageously have a content of cyclic or linear silicone oils or consist entirely of such oils, although it is preferable to use an additional content of their oil phase components apart from the silicone oil or silicone oils.

Cyclomethione (octamethylcyclotetrasiloxane) is advantageously used as silicone oil to be used according to the present invention. However, other silicone oils can also be used advantageously for the purposes of the present invention, for example, hexamethylcyclotrisiloxane, polydimethylsiloxane, poly(methylphenylsiloxane).

Also advantageous are mixtures of cyclomethicone and isotridecyl isononanoate, and of cyclomethicone and 2-ethylhexyl isostearate.

The aqueous phase of the preparations according to the present invention optionally advantageously comprises alcohols, diols or polyols (lower alkyl), and ethers thereof, preferably ethanol, isopropanol, propylene glycol, glycarol, ethylene glycol-monoethyl or monobutyl ether, propylene glycol monomethyl, -monoethyl or monobutyl ether, diethylene glycol monomethyl or -monoethyl ether and analogous products, and also alcohols (lower alkyl), e.g. ethanol, 1,2-propanediol, glycerol, and, in particular, one or more thickeners which can advantageously be chosen from the group of silicon dioxide, aluminum silicates, polysaccarides and derivatives thereof, e.g. hyaluronic acid, xanthan gum, hydroxypropylmethylcellulose, particularly advantageously from the group of polyacrylates, preferably a polyacrylate from the group of so-called Carbopols, for example, Carbopol grades 980, 981, 1382, 2084, 5984, in each case individually or in combination.

A comprehensive description of the raw materials and active ingredients used in cosmetic compositions is given in DE-A 199 19 630.

It could not have been foreseen that the indanylidene compounds according to the present invention represent an excellent selection compared with the compounds known from EP-A 823 418.

EXAMPLES

Photostability

By way of example, comparative measurements is between the compounds of category A and the compounds of category B and the combination with other standard commercial UV filters such as OMC (=octyl methoxycinnamate) or BMDM (=tert-butylmethoxydibenzoylmethane) are listed below. The substances of category B demonstrate the improvement over the substances of category A. The irradiation was carried out in a Suntester from Heraeus at an irradiation intensity of 765 W/m² (based on Global sensor). The values give the concentration decrease of the UV filters in percentage following irradiation (dose in J/cm²).

Formulation according to formulation Example 1: TABLE 1 Compound A1 A2 B1 B2 B3  72 J/cm² 10% 1% 2% 1% 1% 144 J/cm² 13% 6% 3% 2% 2%

Formulation according to formulation Example 12 TABLE 2 Combination A1 OMC A2 OMC B1 OMC B2 OMC B3 OMC  72 J/cm² 22% 27% 14%  7% 2% 12% 6% 11% 6% 11% 144 J/cm² 37% 35% 26% 12% 3% 19% 6% 13% 6% 13%

TABLE 3 Formulation according to: Comparison Example Example 4 without A or B 12 without OMC Example 4 Combination OMC BMDM B3 OMC B3 BMDM B3 OMC BMDM  72 J/cm² 48% 68% 6% 11% 2%  5% 3% 17% 35% 144 J/cm² 59% 85% 6% 13% 3% 13% 5% 26% 54%

Compounds in Tables 1-3

Example 1 2-(5,6-Dimethoxy-3,3-dimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile

44 g (0.2 mol) of 5,6-dimethoxy-3,3-dimethyl-1-indanone, 25 g (0.2 mol) of pivaloylacetonitrile, 32 g of propionic acid and 17 g of ammonium acetate are mixed in 80 g of xylene and heated at 120° C. for 7 hours. After the system has been cooled to room temperature and the organic phase has been washed, the xylene is distilled off, and the crude product which remains is recrystallized in methanol. Yield: 50% theory; E^(1/1) 730 (λ_(max) 373 nm).

Example 2 2-(5-Methoxy-3,3,4,6-tetramethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile

The procedure was analogous to that in Example 1 starting from 5-methoxy-3,3,4,6-tetramethyl-1-indanone. Yield: 50% of theory; E^(1/1) 588 (λ_(max) 340 nm).

Example 3 2-(3,3,5,6-tetramethyl-1-indanylidene-4,4-dimethyl-3-oxo-pentanonitrile

The procedure was analogous to that in Example 1 starting from 3,3,5,6-tetramethyl-1-indanone. Yield: 55% of theory; E^(1/1) 630 (λ_(max) 342 nm).

Example 4 2-(3,3,6-trimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile

The procedure was analogous to that in Example 1 starting from 3,3,6-trimethyl-1-indanone. Yield: 45% of theory; E^(1/1) 528/505 (λ_(max) 335/316 nm).

Example 5 2-(5,6-Ethylenedioxo-3,3-dimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile

The procedure was analogous to that in Example 1 starting from 5,6-ethylenedioxo-3,3-dimethyl-1-indanone. Yield: 55% of theory; E^(1/1) 640 (λ_(max) 369 nm).

Example 6 2-(5-Methoxy-3,3,6-trimethyl-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile

The procedure was analogous to that in Example 1 starting from 5-methoxy-3,3,6-trimethyl-1-indanone. Yield: 60% of theory; E^(1/1) 850 (λ_(max) 359 nm).

Example 7 2-[{5-Methoxy-3,3-dimethyl-(2-methyl-3-(1,3,3,3-tetramethyl-1-(trimethyl-silyloxy)-disiloxanyl}-propyl)-indanylidene)]-4,4-dimethyl-3-oxo-pentanonitrile

a) 2-(5-Methoxy-3,3-dimethyl-6-hydroxy-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile

5-Methoxy-3,3-dimethyl-6-hydroxy-1-indanone is reacted according to Example 1. Yield: 50% of theory. b) 2-(5-Methoxy-3,3-dimethyl-6-(2-methyl-propenyloxy)-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile

136 g (0.43 mol) of the compound under a) are added together with 95 g of potassium carbonate to 470 g of N-methylpyrrolidinone, heated to 70° C. and 42 g (0.46 mol) of methallyl chloride are added thereto over the course of 30 min. The mixture is heated for a further 3 h at 70° C., then cooled to room temperature, and the product is extracted with ethyl acetate. Yield: 45% of theory.

90 g (130 mmol) of the compound under b), 29 g (130 mmol) of 1,1,3,5,5,5-heptamethyltrisiloxane are kept at 80° C. in the presence of catalytic amounts of divinyltetramethylplatinum complex in 90 g of toluene and a nitrogen atmosphere for 20 h. After the solvent has been distilled off, the residue is distilled over a Kugelrohr, giving 50 g (70% of theory) of the desired product as a yellow oil; E^(1/1) 400 (λ_(max) 373 nm).

Example 8 2-(6-Acetoxy-3,3-dimethyl-5-methoxy-1-indanylidene)-4,4-dimethyl-3-oxo-pentanonitrile

54 g (0.17 mol) of the compound under a) are reacted with 13 g (0.17 mol) of acetyl chloride in N-methylpyrrolidinone at 40° C. over the course of 5 h. Yield: 98% of theory.

E^(1/1) 420/280 (λ_(max) 355/302 nm).

Example 9 2-(3,3-Dimethyl-5-tert-butyl-1-indanylidene)-3-(1′-methylcyclohexyl)-3-oxo-propiononitrile

3,3-Dimethyl-5-tert-butyl-1-indanone are reacted with 3-(1′-methylcyclohexyl)-3-oxo-propionitrile analogously to Example 1.

-   Yield: 40% of theory. -   E^(1/1) 580 (λ_(max) 355 nm).

Example 10 2-(3,3,5-Trimethyl-1-indanylidene)-3-phenyl-3-oxo-propionitrile

3,3,5-Trimethyl-1-indanone are reacted with benzoylacetonitrile analogously to Example 1.

-   Yield: 50% of theory. -   E^(1/1) 600 (λ_(max) 350 nm).

Formulation Example 1

Sunscreen soft cream (O/W), in-vitro SPF 3, water resistant TABLE 4 Part Raw Materials INCI Name % (wt.) A Crodafos MCA Cetyl Phosphate 1.50 Cutina MD Glyceryl Stearate 2.00 Copherol 1250 Tocopheryl Acetate 0.50 Lanette 16 Cetyl Alcohol 1.00 Tegosoft TN C 12-15 Alkyl 24.00 Benzoate Prisorine 3505 Isostearic Acid 1.00 UV absorber according to 3.00 formula I B Water, dist. Water (Aqua) 59.60 EDETA B liq. Tetrasodium EDTA 0.20 Glycerol, 99% Glycerin 3.00 Phenoxyethanol Phenoxyethanol 0.70 Solbrol M Methylparaben 0.20 Solbrol P Propylparaben 0.10 Carbopol ETD 2050 Carbomer 0.20 C Sodium hydroxide solution, Sodium Hydroxide 2.70 10% aq. D Perfume oil Parfum (Fragrance) 0.30 Preparation Method

-   Part A: Heat to about 85° C. -   Part B: Weigh in raw materials without Carbopol. Disperse Carbopol     therein using Ultra Turrax. Heat to about 85° C. Add B to A. -   Part C: Immediately add to A/B and then homogenize while hot (Ultra     Turrax). Leave to cool with stirring.

Part D: Add and stir in. TABLE 5 in-vitro SPF (Labsphere Ultraviolet Transmittance Analyzer) 3 Boots star rating 4 Broad spectrum rating (Diffey) 4 Critical wavelength (90% absorption at λ in nm) 385 UV filter substantivity after watering 97%

Formulation Example 2

Sunscreen Lotion (O/W), In-vitro SPF 20 TABLE 6 Part Raw Materials INCI Name % (wt.) A Crodafos MCA Cetyl Phosphate 1.50 Cutina MD Glyceryl Stearate 2.00 Copherol 1250 Tocopheryl Acetate 0.50 Lanette 16 Cetyl Alcohol 1.00 Tegosoft TN C 12-15 Alkyl 10.60 Benzoate Prisorine 3505 Isostearic Acid 1.00 UV absorber according to 2.00 formula I Neo Heliopan ® AV Ethylhexyl 5.00 Methoxycinnamate B Water, dist. Water (Aqua) 55.07 EDETA B fl. Tetrasodium EDTA 0.20 Glycerol, 99% Glycerin 3.00 Phenoxyethanol Phenoxyethanol 0.70 Solbrol M Methylparaben 0.20 Solbrol P Propylparaben 0.10 Carbopol ETD 2050 Carbomer 0.20 C Sodium hydroxide solution, Sodium hydroxide 3.30 10% aq. Neo Hellopan ® Hydro, Phenylbenzimidazole 13.33 15% strength solution Sulfonic Acid neutralized with NaOH D Perfume oil Parfum (Fragrance) 0.30 Preparation Method

-   Part A: Heat to about 85° C. -   Part B: Weigh in raw materials without Carbopol. Disperse Carbopol     therein using Ultra Turrax. Heat to about 85° C. Add B to A. -   Part C: Immediately add to A/B and then homogenize while hot (Ultra     Turrax). Leave to cool with stirring.

Part D: Add and stir in. TABLE 7 in-vitro SPF (Labsphere Ultraviolet Transmittance Analyzer) 20 Boots star rating 2 Broad spectrum rating (Diffey) 4 Critical wavelength (90% absorption at λ in nm) 378

Formulation Example 3

Sunscreen Milk (O/W), In-Vitro SPF 6 TABLE 8 Part Raw Materials INCI Name % (wt.) A Tegin M Glyceryl Stearate 2.50 Tagat S PEG-30 Glyceryl Stearate 1.95 Lanette O Cetearyl Alcohol 2.20 Copherol 1250 Tocopheryl Acetate 0.50 Miglyol 8810 Butylene Glycol Dicaprylate/ 12.00 Caprate Tegosoft TN C12-C15 Alkyl Benzoate 8.00 Phenonip Phenoxyethanol (and) 0.15 methylparaben (and) Butylparaben (and) ethylparaben (and) Propylparaben UV absorber 5.00 according to formula I B Water, dist. Water (Aqua) 43.90 EDETA BD Disodium EDETA 0.10 1,2-Propylene Propylene Glycol 2.00 glycol Phenonip Phenoxyethanol (and) 0.30 Methylparaben (and) Butylparaben (and) Ethylparaben (and) Propylparaben C Water, dist. Water (Aqua) 19.00 Carbopol 2050 Carbomer 0.40 NaOH, 10% strength Sodium Hydroxide 1.70 D Perfume oil Parfum (Fragrance) 0.30 Preparation Method

-   Part A: Heat to 80-85° C. -   Part B: Heat to 80-85° C., add part B to part A with stirring. -   Part C: Disperse Carbopol into the water and neutralize with NaOH,     with stirring. Add part C at about 60° C. with stirring. Allow to     cool at RT. -   Part D: Add and stir.

Formulation Example 4 TABLE 9 in-vitro SPF (Labsphere Ultraviolet Transmittance Analyzer) 6 Boots Star Rating 4 Broad Spectrum Rating (Diffey) 4 Critical wavelength (90% absorption at λ in nm) 385

Sunscreen Lotion (O/W), In-vitro SPF 21 TABLE 10 Part Raw Materials INCI Name % (wt.) A Tegin M Glyceryl Stearate 2.50 Tagat S PEG-30 Glyceryl Stearate 1.95 Lanette O Cetearyl Alcohol 2.20 Copherol 1250 Tocopheryl Acetate 0.50 Miglyol 8810 Butylene Glycol Dicaprylate/ 12.00 Caprate Tegosoft TN C12-C15 Alkyl Benzoate 8.00 Phenonip Phenoxyethanol (and) 0.20 Methylparaben (and) Butylparaben (and) Ethylparaben (and) Propylparaben UV absorber 2.00 according to formula I Neo Heliopan ® AV Ethylhexyl 5.00 methoxycinnamate Neo Heliopan ® 357 Butyl 1.00 methoxydibenzoylmethane B Water, dist. Water (Aqua) 39.35 EDETA BD Disodium EDETA 0.10 1,2- Propylene Glycol 2.00 Propyleneglycol Phenonip Phenoxyethanol (and) 0.30 Methylparaben (and) Butylparaben (and) Ethylparaben (and) Propylparaben Vitamin C Ascorbic Acid 0.10 C Water, dist. Water (Aqua) 20.00 Carbopol 2050 Carbomer 0.40 NaOH, 10% strength Sodium Hydroxide 1.70 D Perfume oil Parfum (Fragrance) 0.30 Preparation Method

-   Part A: Heat to 80-85° C. -   Part B: Heat to 80-85° C., add part B to part A with stirring. -   Part C: Disperse Carbopol into the water and neutralize with NaOh,     with stirring. -    Add part C at about 60° C. with stirring. Allow to cool to RT.

Part D: Add and stir. TABLE 11 in-vitro SPF (Labsphere Ultraviolet Transmittance Analyzer) 21 Boots Star Rating 3 Broad Spectrum Rating (Diffey) 4 Critical wavelength (90% absorption at λ in nm) 379

Formulation Example 5

Sunscreen Lotion (O/W), In-vitro SPF 11 TABLE 12 Part Raw Materials INCI Name % (wt.) A Eumulgin VL 75 Lauryl Glucoside (and) 3.00 Polyglyceryl-2- Dipolyhydroxystearate (and) Glycerin Tegosoft TN C12-C15 Alkyl Benzoate 20.00 Copherol 1250 Tocopheryl Acetate 0.50 UV absorber according 3.00 to formula I Perfume oil Parfum (Fragrance) 0.20 Neo Heliopan ® 303 Octocrylene 5.00 Carbopol 2984 Carbomer 0.35 Pemulen TR-1 Acrylates/C10-30 Alkyl 0.15 Acrylate Crosspolymer B Water, dist. Water (Aqua) 60.50 EDETA BD Disodium EDTA 0.10 Glycerol, 99% Glycerin 5.00 Phenoxyethanol Phenoxyethanol 0.70 Solbrol M Methylparaben 0.20 Solbrol P Propylparaben 0.10 C NaOH, 10% strength Sodium Hydroxide 1.20 Preparation Method

-   Part A: Dissolve UV absorber according to formula I in the oils or     liquid UV filters (heating to about 70° C.). Allow to cool to about     30° C., add the remaining constituents apart from Carbopol and     Pemulen and mix at room temperature (stir for about 5 minutes). Stir     in Carbopol and Pemulen. -   Part B: Dissolve Salbrols in phenoxyethanol with heating. Mix with     water and glycerol, add to part A with stirring. Stir for about 60     minutes.

Part C: Add to A/B, homogenize using the Ultra Turrax. TABLE 13 in-vitro SPF (Labsphere Ultraviolet Transmittance Analyzer) 11 Boots Star Rating 4 Broad Spectrum Rating (Diffey) 4 Critical wavelength (90% Absorption at λ in nm) 382

Formulation Example 6

Sunscreen Cream (W/O), In-vitro SPF 4, Water Resistant TABLE 14 Part Raw Materials INCI Name % (wt.) A Dehymuls PGPH Polyglyceryl-2 5.00 Dipolyhydroxystearate Copherol 1250 Tocopheryl Acetate 0.50 Permulgin 3220 Ozokerite 0.50 Zinc stearate Zinc Stearate 0.50 Tegosoft TN C12-15 Alkyl Benzoate 25.00 UV absorber according 5.00 to formula I B Water, dist. Water (Aqua) 57.90 EDETA BD Disodium EDTA 0.10 Glycerol, 99% Glycerin 4.00 Phenoxyethanol Phenoxyethanol 0.70 Solbrol M Methylparaben 0.20 Solbrol P Propylparaben 0.10 Magnesium sulfate Magnesium Sulfate 0.50 Preparation Method

-   Part A: Heat to about 85° C. -   Part B: Heat to about 85° C. (without zinc oxide; dispense zinc     oxide therein using the Ultra Turrax. -    Add B to A.

 Allow to cool with stirring, then homogenize. TABLE 15 in-vitro SPF (Labsphere Ultraviolet Transmittance Analyzer) 4 Boots Star Rating 4 Broad Spectrum Rating (Diffey) 4 Critical wavelength (90% Absorption at λ in nm) 384 UV filter substantivity after watering 95%

Formulation Example 7

Sunscreen Softcream (W/O), In-vitro SPF 40 TABLE 16 Part Raw Materials INCI Name % (wt.) A Dehymuls PGPH Polyglyceryl-2 5.00 Dipolyhydroxystearate Copherol 1250 Tocopheryl Acetate 0.50 Permulgin 3220 Ozokerite 0.50 Zinc stearate Zinc Stearate 0.50 Tegosoft TN C12-15 Alkyl Benzoate 10.00 UV absorber according 2.00 to formula I Neo Heliopan ® 303 Octocrylene 5.00 Neo Heliopan ® MBC 4-Methylbenzylidene 3.00 Camphor Zinc oxide neutral H&R Zinc Oxide 5.00 B Water, dist. Water (Aqua) 62.90 EDETA BD Disodium EDTA 0.10 Glycerol, 99% Glycerin 4.00 Phenoxyethanol Phenoxyethanol 0.70 Solbrol M Methylparaben 0.20 Solbrol P Propylparaben 0.10 Magnesium sulfate Magnesium Sulfate 0.50 C Parfume oil Parfum (Fragrance) 0.20 Preparation Method

-   Part A: Heat to about 85° C. -   Part B: Heat to about 85° C. (without zinc oxide; disperse zinc     oxide therein using the Ultra Turrax). -    Add B to A. -    Allow to cool with stirring.

Part C: Add and then homogenize. TABLE 17 in-vitro SPF (Labsphere Ultraviolet Transmittance Analyzer) 40 Boots Star Rating 3 Broad Spectrum Rating (Diffey) 4 Critical wavelength (90% Absorption at λ in nm) 379

Formulation Example 8

Sunscreen Milk (W/O) TABLE 18 Part Raw Materials INCI Name % (wt.) A Dehymuls PGPH Polyglyceryl-2 3.00 Dipolyhydroxystearate Beeswax 8100 Beeswax 1.00 Monomuls 90-0-18 Glyceryl Oleate 1.00 Zinc stearate Zinc Stearate 1.00 Cetiol SN Cetearyl Isononanoate 5.00 Cetiol OE Dicaprylyl Ether 5.00 Tegosoft TN C12-15 Alkyl Benzoate 4.00 Copherol 1250 Tocopheryl Acetate 0.50 Solbrol P Propylparaben 0.10 Neo Heliopan ® OS Ethylhexyl Salicylate 5.00 Neo Heliopan ® AV Ethylhexyl 7.50 Methoxycinnamate UV absorber according 1.50 to formula I B Water, dist. Water (Aqua) 44.10 Trilon BD Disodium EDTA 0.10 Glycerol, 99% Glycerin 5.00 Solbrol M Methylparaben 0.20 Phenoxyethanol Phenoxyethanol 0.70 Neo Heliopan ® AP 10% Disodium Phenyl 15.00 strength solution Dibenzimidazole neutralized with NaOH Tatrasulfonate C Perfume oil Parfum (Fragrance) 0.30 Bisabolol Bisabolol 0.10 Preparation Method

-   Part A: Heat to about 85° C. -   Part B: Heat to about 85° C. Add B to A. Allow to cool with     stirring. -   Part C: Add and then homogenize.

Formulation Example 9

Daycare Cream with UV Protection TABLE 19 Part Raw Materials INCI Name % (wt.) A Emulgade PL 68/50 Cetearyl Glycoside (and) 4.50 Cetearyl Alcohol Cetiol PGL Hexyldecanol (and) 8.00 Hexyldecyl Laurate Myritol 331 Cocoglycerides 8.00 Copherol 1250 Tocopheryl Acetate 0.50 Neo Heliopan ® E1000 Isoamylp- 2.00 Methoxycinnamate UV absorber according 2.00 to formula I B Water, dist. Water (Aqua) 45.40 Glycerol Glycerin 3.00 Phenonip Phenoxyethanol (and) 0.50 Methylparaben (and) Butylparaben (and) Ethylparaben (and) Propylparaben C Water, dist. Water (Aqua) 25.00 Carbopol ETD 2050 Carbomer 0.20 NaOH, 10% strength Sodium Hydroxide 0.60 Perfume oil Parfum (Fragrance) 0.30 Preparation Method

-   Part A: Heat to 80° C. -   Part B: Heat to 80° C. to part A with stirring. -   Part C: Disperse Carbopol in water and neutralize with sodium     hydroxide solution. Add to part A/B at about 55° C. -   Part D: Add at RT and homogenize.

Formulation Example 10

Sunscreen Spray TABLE 20 Part Raw Materials INCI Name % (wt.) A Water, demin. Water (Aqua) 69.50 Glycerol, 99% Glycerin 4.00 1,3 Butylene glycol Butylene Glycol 5.00 D-Panthenol Panthenol 0.50 Lara Care A-200 Galactoarabinan 0.25 B Baysilone oil M 10 Dimethicone 1.00 Edeta BD Disodium EDTA 0.10 Copherol 1250 Tocopheryl Acetate 0.50 Cetiol OE Dicaprylyl Ether 3.00 Neo Heliopan ® HMS Homosalate 5.00 Neo Heliopan ® AV Ethylhexyl 6.00 Methoxycinnamate Neo Heliopan ® 357 Butyl 1.00 Methoxydibenzoylmethane UV absorber 2.00 according to formula I alpha-bisabolol Bisabolol 0.10 nat. H&R Pemulen TR-2 Acrylates/C10-30 Alkyl 0.25 Acrylate Crosspolymer C Phenoxyethanol Phenoxyethanol 0.70 Solbrol M Methylparaben 0.20 Solbrol P Propylparaben 0.10 D NaOH, 10% strength Sodium Hydroxide 0.60 E Perfume oil Fragrance (Parfum) 0.20 Preparation Method

-   Part A: Dissolve Lara Care A-200 into the other constituents of part     A with stirring. -   Part B: Weigh in all raw materials (without Pemulen) and dissolve     the crystalline substances with heating. Dispense Pemulen therein.     Add part B to part A then homogenize for 1 minute. -    Add part C+D and homogenize again for 1-2 minutes using the Ultra     Turrax.

Formulation Example 11

Sunscreen Hydrodispersion Gel (Balm) TABLE 21 Part Raw Materials INCI Name % (wt.) A Water, dist. Water (Aqua) 74.90 Carbopol 1342 Acrylates/C10-30 Alkyl 1.00 Acrylate Crosspolymer Triethanolamine Triethanolamine 1.20 B Neo Heliopan ® Hydro, Phenylbenzimidazole 10.00 30% strength solution Sulfonic Acid neutralized with TEA C Neo Heliopan ® AV Ethylhexyl 3.00 Methoxycinnamate UV absorber according 2.00 to formula I Isopropyl myristate Isopropyl Myristate 4.00 Baysilone oil PK 20 Phenyl Trimethicone 3.00 Phenonip Phenoxyethanol (and) 0.50 Methylparaben (and) Butylparaben (and) Ethylparaben (and) Propylparaben Perfume oil Parfum (Fragrance) 0.30 Bisabolol nat. H&R Bisabolol 0.10 Preparation Method

-   Part A: Disperse Carbopol in water and neutralize with sodium     hydroxide solution. -   Part B: Add to part A with stirring. -   Part C: Dissolve crystalline constituents in the other raw materials     of part C with warming (max 40° C.) and add to part A/B. Stir well     and then homogenize. (Homozenta).

Formulation Example 12

Hair Conditioner with UV Filters TABLE 22 Part Raw Materials INCI Name % (wt.) A Emulgade 1000 NI Cetearyl Alcohol (and) 2.00 Ceteareth-20 Lanette 16 Cetyl Alcohol 1.00 Neo Heliopan ® AV 2-Ethylhexyl 3.00 Methoxycinnamate UV absorber according 1.00 to formula I B Water, dist. Water (Aqua) 91.70 Edeta BD Disodium EDTA 0.10 Phenonip Phenoxyethanol (and) 0.40 Methylparaben (and) Butylparaben (and) Ethylparaben (and) Propylparaben Dehyquart A-CA Cetrimonium Chloride 0.20 NaOH, 1% strength Sodium Hydroxide 0.30 Perfume oil Parfum (Fragrance) 0.30 Preparation Method

-   Part A: Heat to 80° C. -   Part B: Heat to 80° C. Add to part A with stirring. -   Part C: Add at 40° C. and cool to RT.

Formulation Example 13

Sunscreen Lotion (O/W) TABLE 23 Part Raw Materials INCI Name % (wt.) A Tegin M Glyceryl Stearate 2.50 Tagat S PEG-30 Glyceryl Stearate 1.95 Lanette O Cetearyl Alcohol 2.20 Hallbrite TQ Diethylhexyl Naphthalate 7.00 Cetiol B Dibutyl Adipate 5.00 Tegosoft TN C12-C15 Alkylbenzoate 4.00 Myritol PC Propylene Glycol 4.00 Dicaprylate/Dicaprate Phenonip Phenoxyethanol (and) 0.15 Methylparaben (and) Butylparaben (and) Ethylparaben (and) Propylparaben UV absorber according 2.00 to formula I Neo Heliopan ® AV Ethylhexyl 5.00 Methoxycinnamate B Water, dist. Water (Aqua) 42.80 1,2-Propylene glycol Propylene Glycol 2.00 Phenonip Phenoxyethanol (and) 0.30 Methylparaben (and) Butylparaben (and) Ethylparaben (and) Propylparaben C Water, dist. Water (Aqua) 19.00 Carbopol 2050 Carbomer 0.40 NaOH, 10% strength Sodium Hydroxide 1.70 Preparation method

-   Part A: Heat to 80-85° C. -   Part B: Heat to 80-85° C., add part B to part A with stirring. -   Part C: Disperse Carbopol into the water and neutralize with NaOH     with stirring. Add part C at about 60° C. with stirring.

Although the invention has been described in detail in the foregoing for the purpose of illustration, it is to be understood that such detail is solely for that purpose and that variations can be made therein by those skilled in the art without departing from the spirit and scope of the invention except as it may be limited by the claims. 

1-17. (canceled)
 18. Indanone compounds of the formula: 